Canonical Allele Identifier: PA2830123097
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447399
ClinVar RCV Id: RCV000518632 RCV002464020 RCV003403214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe147Ile
CA367401967
NM_033508.3:c.439T>A